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Donations Available Until 19th April 2018
David Shan
6y
€50
Nicola C
6y
€50
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Please support my challenge to the Arctic Circle in aid of Debra Ireland. Debra Ireland are a charity that help children with a severe,rare,genetic skin condition known as EB-Epidermolysis Bullosa(Butterfly skin) The children are born with no collagen holding their skin together; their whole bod...
Please support my challenge to the Arctic Circle in aid of Debra Ireland. Debra Ireland are a charity that help children with a severe,rare,genetic skin condition known as EB-Epidermolysis Bullosa(Butterfly skin) The children are born with no collagen holding their skin together; their whole bodies have to be covered in bandages to protect their skin and every second day they have to undergo a 3½ hour dressing change to protect their delicate skin. The slightest touch can cause blisters all over their body. There are only 300 people with this skin condition in Ireland and sadly 3 children under the age of 8 passed away this year.I have met some amazing people with EB and I have been truly touched by their bravery and outlook on life.
Therefore..in March next, 2018, I will be undertaking a very big challenge. 18 of us brave Irish women are participating in “The Arctic Challenge” for Debra Ireland. The challenge will involve surviving the extreme cold of the Arctic region, learning survival skills in this harsh environment, ski skills, pulling a sled through deep snow, camping out overnight in sub-zero temperatures etc. I have to raise over €5,000 for this challenge - all of which will go to Debra Ireland.This will make a HUGE difference to the charity as unfortunately Debra Ireland receive no state funding and therefore rely on contributions such as this. Money raised goes towards nursing and medical care.
PLEASE PLEASE support my challenge to the Arctic and help those with EB in Ireland.
Thank you,Sarah x
Artic Challenge 2018 For DEBRA Ireland
Congrats Sarah & Team! Up the Naaaaaaavan! :)
Good Luck Sarah....no doubt you will ace it and all the hard training will pay off. Can’t wait to hear all the stories. Niamh Xx
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We might be a small charity but, make no mistake, our mission and our ambitions are colossal. We are here to tell Ireland and the world beyond its borders about Epidermolysis Bullosa. We are here to compel everyone to care and inspire everyone to act. We are here to be a positive force for all those living with EB and all those whose lives have been impacted by EB. To help in all kinds of everyday ways, to listen, support, empower and alleviate unimaginable pressures. We are here to lobby tho
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